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JPS5988719A - Polyester film for base material of liquid crystal panel - Google Patents

Polyester film for base material of liquid crystal panel

Info

Publication number
JPS5988719A
JPS5988719A JP20003782A JP20003782A JPS5988719A JP S5988719 A JPS5988719 A JP S5988719A JP 20003782 A JP20003782 A JP 20003782A JP 20003782 A JP20003782 A JP 20003782A JP S5988719 A JPS5988719 A JP S5988719A
Authority
JP
Japan
Prior art keywords
film
polyester
polyester film
thickness
liquid crystal
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP20003782A
Other languages
Japanese (ja)
Other versions
JPH0466002B2 (en
Inventor
Shigeo Uchiumi
滋夫 内海
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Diafoil Co Ltd
Original Assignee
Diafoil Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Diafoil Co Ltd filed Critical Diafoil Co Ltd
Priority to JP20003782A priority Critical patent/JPS5988719A/en
Publication of JPS5988719A publication Critical patent/JPS5988719A/en
Publication of JPH0466002B2 publication Critical patent/JPH0466002B2/ja
Granted legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G02OPTICS
    • G02FOPTICAL DEVICES OR ARRANGEMENTS FOR THE CONTROL OF LIGHT BY MODIFICATION OF THE OPTICAL PROPERTIES OF THE MEDIA OF THE ELEMENTS INVOLVED THEREIN; NON-LINEAR OPTICS; FREQUENCY-CHANGING OF LIGHT; OPTICAL LOGIC ELEMENTS; OPTICAL ANALOGUE/DIGITAL CONVERTERS
    • G02F1/00Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics
    • G02F1/01Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour 
    • G02F1/13Devices or arrangements for the control of the intensity, colour, phase, polarisation or direction of light arriving from an independent light source, e.g. switching, gating or modulating; Non-linear optics for the control of the intensity, phase, polarisation or colour  based on liquid crystals, e.g. single liquid crystal display cells
    • G02F1/133Constructional arrangements; Operation of liquid crystal cells; Circuit arrangements
    • G02F1/1333Constructional arrangements; Manufacturing methods

Landscapes

  • Physics & Mathematics (AREA)
  • Nonlinear Science (AREA)
  • Liquid Crystal (AREA)
  • Mathematical Physics (AREA)
  • Chemical & Material Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • General Physics & Mathematics (AREA)
  • Optics & Photonics (AREA)

Abstract

PURPOSE:To provide a polyester film made of terephthalate- or 2,6-naphtalate- polyester which has a specified birefringence index and haze and is improved in the coloring due to interference fringes. CONSTITUTION:The polyester film of this invention is made of terephthalate- or 2,6-naphtalate-polyester and has a birefringence index of 30X10<-3>-110X10<-3>, a thickness of 100mum, and a haze of <=5%. It is desirable to use a polyester whose transparency is not lowered and dimensions are not changed when heated, since the film is put in a heated condition at the time of manufacturing liquid crystal panels. It is desirable from the point of practical use that the coefficient of contraction is <=5% when held in a 150 deg.C atmosphere for 30min and the haze is <=5% at a thickness of 100mum. These conditions are achieved when a film of >=30X10<-3> in the degree of surface orientation is heat treated so that its mean refractive index becomes >=1.595 in the manufacturing process of the film.

Description

【発明の詳細な説明】 本発明は液晶パネル基材用ポリエステルフィルムに関す
るものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a polyester film for liquid crystal panel substrates.

液晶パネル基材としては、従来からガラス板がもっばら
用いられてきた。ガラス板は性能的には優れた基材であ
るが、衝撃に対して脆く。
Glass plates have traditionally been widely used as liquid crystal panel substrates. Although glass plates are excellent base materials in terms of performance, they are brittle against impacts.

かつ機械的強度の点よシして薄くすることが困難である
。従ってガラス板の代シにプラスチックフィルムを液晶
パネルの基材として用いることが検討されている。グラ
スチックフィルムを基材とする液晶パネルは、可撓性、
軽量性、加工性、耐衝撃性、薄型化など、ガラスでは達
成できない特性を発揮することが期待される。
Moreover, it is difficult to make it thin due to the mechanical strength. Therefore, the use of plastic films as base materials for liquid crystal panels in place of glass plates is being considered. Liquid crystal panels based on glass film are flexible,
It is expected to exhibit properties that cannot be achieved with glass, such as lightness, processability, impact resistance, and thinness.

液晶パネル基材用のグラスチックフィルムには各種のも
のが提案されているが、耐熱性、耐湿性、耐薬品性、機
械的強度等の点よりしてテレフタレートまたはコ、6−
ナフタレート系ボリエステルが有望である。
Various types of glass films have been proposed for use as substrates for liquid crystal panels, but from the viewpoint of heat resistance, moisture resistance, chemical resistance, mechanical strength, etc.
Naphthalate polyesters are promising.

液晶ハネル基材用のプラスチックフィルムは。Plastic film for LCD panel substrates.

パネルとしての適正視角を狭めず、かつ液晶表示装置と
しての判読性を低下させないものでなければならない。
It must be something that does not narrow the appropriate viewing angle as a panel and does not reduce readability as a liquid crystal display device.

そのためにはフィルムを一枚の偏光板で挾んだときに、
どの方向から見ても干渉縞が発生しないことが必要であ
る。従来、この条件ケ渦足させるためには、フィルムの
レターデーシヨン値(R値)がrOmμ以下であること
が必要とされていた(%開昭57−//f、220号公
報参照)。
To achieve this, when the film is sandwiched between two polarizing plates,
It is necessary that no interference fringes occur when viewed from any direction. Conventionally, in order to satisfy this condition, it has been necessary that the retardation value (R value) of the film be less than rOmμ (see Publication No. 220, 1987-//f).

しかし1本発明者の検討によれば、テレフタレートまた
はコツ6−ナフタレート系ポリエステルのフィルムを基
材とする液晶パネルでは、フィルムのR値が!θmμ以
下の楊会には%真上から見たときには干渉縞が無くても
、方向を変えて見ると干渉縞による着色があることが判
明した。本発明者はこの点について検討した結果。
However, according to the inventor's study, in a liquid crystal panel based on a terephthalate or naphthalate polyester film, the R value of the film is! It has been found that even though there are no interference fringes when viewed from directly above, there is coloring due to interference fringes when viewed from a different direction in the Yang Kai below θmμ. This is the result of the inventor's study on this point.

篤くべきことに、高配向させた、すなわちR値の大きい
フィルムを、偏光板の偏光軸とフィルムの玉軸とが一致
するようにパネルに組込んだならば、いかなる方向から
見ても干渉縞による岩色が発生しないことを見出し5本
発明を完成した。
In particular, if a highly oriented film, that is, a film with a large R value, is assembled into a panel so that the polarization axis of the polarizing plate and the ball axis of the film coincide, interference fringes will be generated when viewed from any direction. The present invention was completed based on the discovery that no rock color occurs due to

すなわち1本発明の要旨は、テレフタレートまたはコツ
6−ナフタレート系ポリエステルよりなり、複屈折率が
3θ×/θ−3〜//θ×/θ4であり、かつiooμ
の厚さでのヘーズが!係以下であることを特徴とする液
晶パネル基材用ポリエステルフィルムに存スル。
That is, the gist of the present invention is that it is made of terephthalate or naphthalate polyester, has a birefringence of 3θ×/θ−3 to //θ×/θ4, and has an iooμ
Haze at a thickness of ! The present invention relates to polyester films for LCD panel substrates, which are characterized by having a polyester film of less than 10%.

本発明について詳細に説明すると、本発明で用いるテレ
フタレートまたはコツ6−ナフタレート系ポリエステル
とは、テレフタルvtたハコ、6−ナフタレンジカルボ
ン酸を主たる酸成分とし、エチレングリコールを主たる
グリコール成分とするポリエステルである。テレフタル
酸およびコ、に一ナフタレンジカルボン酸の一部は、イ
ソフタル酸、7タル酸、アジピン酸、セバシン酸。
To explain the present invention in detail, the terephthalate or 6-naphthalate polyester used in the present invention is a polyester containing terephthalate, 6-naphthalene dicarboxylic acid as the main acid component and ethylene glycol as the main glycol component. . Some of the terephthalic acid and di-naphthalene dicarboxylic acids are isophthalic acid, heptalic acid, adipic acid, and sebacic acid.

コハク酸、p−ヒドロキシ安息香酸、ω−ヒドロキシカ
プロン酸等の多官能のカルボン酸で置 3− 換されていてもよい。同様にエチレングリコールの一部
も、トリメチレングリコール、ヘキサメチレングリコー
ル、シクロヘキサンジメタツール(/、Q ) 、ポリ
エチレングリコール等の多価アルコールで置換されてい
てもよい。通常は+ L/ 7タル酸またはコツ6−ナ
フタレンジカルボン酸成分およびエチレングリコール成
分カ、ソれぞれ?θモル%以上、好ましくr/′i90
モル係以上であるポリエステルを用いる。最も一般的し に用いられるのは、テレフタル酸またはコツ6−ナフタ
レンジカルボン酸成分とエチレングリコールとから製造
されるポリエステルでアル。
It may be substituted with a polyfunctional carboxylic acid such as succinic acid, p-hydroxybenzoic acid, and ω-hydroxycaproic acid. Similarly, a portion of ethylene glycol may also be substituted with a polyhydric alcohol such as trimethylene glycol, hexamethylene glycol, cyclohexane dimetatool (/, Q), polyethylene glycol, or the like. Usually +L/7 talic acid or 6-naphthalene dicarboxylic acid component and ethylene glycol component, respectively? θ mol% or more, preferably r/′i90
A polyester having a molar coefficient or higher is used. The most commonly used polyester is a polyester made from a terephthalic acid or 6-naphthalene dicarboxylic acid component and ethylene glycol.

必然的に混入する成分に加えて、安定剤、紫外線吸収剤
、滑剤などポリエステルフィルムノ製造に際し常用され
ている各種の添加剤を含んでいてもよい。しかし1本発
明に係るフィルムは透明性と表面の平滑性が要求される
ので、ポリエステルとしては粒子を実質的に含まないか
In addition to the components that are necessarily mixed, the film may contain various additives commonly used in the production of polyester films, such as stabilizers, ultraviolet absorbers, and lubricants. However, since the film according to the present invention is required to have transparency and surface smoothness, the polyester should be substantially free of particles.

 4− または極めて微細な粒子のみを含むものが好ましい。こ
のようなポリエステルは1例えばエステル交換反応生成
物の重縮合工程において、エチレンアミドホスフェート
等の燐化合物を添加し、エステル交換触媒として用いた
カルシウムまたはカルシウムおよびリチウムと燐とを含
む微細々粒子を析出させることによシ製造することがで
きる。また、シリカやカオリン等の超微粒子を1粒子を
含まないポリエステルに微量添加する方法によっても透
明性と表面の平滑性に優れたフィルムを与えるポリエス
テルを製造することができる。
4- or those containing only extremely fine particles are preferred. Such polyesters are produced by: 1. For example, in the polycondensation process of transesterification products, a phosphorus compound such as ethyleneamide phosphate is added to precipitate fine particles containing calcium or calcium and lithium and phosphorus, which are used as transesterification catalysts. It can be manufactured by Furthermore, a polyester that provides a film with excellent transparency and surface smoothness can also be produced by adding a small amount of ultrafine particles such as silica or kaolin to a polyester that does not contain any particles.

本発明に係るポリエステルフィルムは、上述のポリエス
テルを用いて通常のフィルム製造方法、すなわち押出機
から溶融ポリエステルをシート状に押出し、これを冷却
ロールに接触させて急冷固化し、次いで延伸したのち熱
固定する方法によ)製造することができる。溶融ポリエ
ステルシートを冷却ロールに接触させる際は。
The polyester film according to the present invention can be produced using the above-mentioned polyester using the usual film manufacturing method, that is, extruding molten polyester into a sheet form from an extruder, bringing it into contact with a cooling roll to rapidly solidify it, then stretching, and then heat setting. can be manufactured by the method of When bringing the molten polyester sheet into contact with the cooling roll.

厚み精度のよいフィルムを高速で製造し得るようにいわ
ゆる静電印加冷却法k i4用することが好ましい(特
公昭37−g/グー号公報参照)。静電印加冷却法は溶
融時の比抵抗の大きいポリエステルには適用し難いので
、ポリエステルトシては溶P1狸詩の比抵抗がオ×/θ
’ 12−cm以下のものを用いるのが好ましい。
In order to produce a film with good thickness accuracy at high speed, it is preferable to use the so-called electrostatic cooling method ki4 (see Japanese Patent Publication No. 37-G/Gu). Since the electrostatic cooling method is difficult to apply to polyester, which has a high specific resistance when melted, the specific resistance of melt P1 Tanukishi is O×/θ for polyester.
' It is preferable to use one with a diameter of 12 cm or less.

延伸および熱固定は、得られるフィルムの被屈折率が3
0×10−3〜/lθ×/θ−3であり、かつ/θθμ
の〃さでのヘーズが!多収下となるように行なう。この
条件は1例えば未延伸フィルムを縦方向に面配向度が3
θ×70””以上でかつ厚み斑の少ないフィルムが得ら
れるまで延伸し、これをテンタークリップで把持して横
延伸をしないで熱固定することによシ達成される。
Stretching and heat setting are performed until the resulting film has a refractive index of 3.
0×10−3 to /lθ×/θ−3, and /θθμ
The haze in the middle of nowhere! Do this so that you can get a high yield. This condition is 1. For example, the degree of plane orientation in the longitudinal direction of an unstretched film is 3.
This is achieved by stretching the film until a film of θ x 70"" or more and with little thickness unevenness is obtained, gripping the film with tenter clips, and heat-setting it without transverse stretching.

面配向度が3θ×70””よシも小さいと、熱固定の際
にフィルムに不均一収縮が発生して厚み斑が大きくなっ
たり1球晶が生成してフィルムが白化したりしやすい。
If the degree of plane orientation is as small as 3θ x 70'', the film tends to undergo non-uniform shrinkage during heat setting, resulting in large thickness unevenness or formation of monospherulites, resulting in whitening of the film.

なお、縦延伸倍率が大きくなりすぎると、延伸方向にさ
け易くなるので注意を要する。これを避けるため、縦方
向に延伸したのち横方向にも若干延伸する方法を採用す
ることもできる。
Note that if the longitudinal stretching ratio becomes too large, it will be easy to avoid in the stretching direction, so care must be taken. In order to avoid this, it is also possible to adopt a method in which the film is stretched in the vertical direction and then slightly stretched in the horizontal direction.

また別法として、縦方向に応力−歪曲線で降伏点を示す
以前の低倍率で延伸し1次いでテンターで横方向に延伸
したのち熱固定して、横方向の屈折率が縦方向の屈折率
よシも大きいフィルムとしてもよい。また、かくして得
られるフィルムは厚み雁が?多収下、特に!多収下であ
ることが好ましい。厚み斑が大きいフィルムは。
Another method is to stretch in the longitudinal direction at a low magnification before reaching the yield point on the stress-strain curve, then stretch in the transverse direction with a tenter, and then heat set, so that the refractive index in the transverse direction is the same as the refractive index in the longitudinal direction. It may also be a large film. Also, how thick is the film thus obtained? Especially under high yield conditions! It is preferable that the yield is high. Films with large thickness unevenness.

フィルム中で艮好な部分を選択して便用しなければなら
ないので不利である。
This is disadvantageous because it is necessary to select and conveniently use parts of the film that are attractive.

フィルムの厚きは70〜!θθμが適当であり、好まし
くは!θ〜200μである。
The thickness of the film is 70~! θθμ is appropriate, preferably! θ~200μ.

薄すぎるフィルムでは、いわゆる1こし”が弱くなるし
、逆に厚すぎると液晶パネルを薄くするという要望にそ
ぐわなくなる。
If the film is too thin, the so-called 1-thickness will be weakened, and if it is too thick, it will not meet the demand for thinner LCD panels.

また、本発明に係るフィルムは、ヘース゛がj多収下で
複屈折率がjOXlo−”〜/10x10−”でなけれ
ばならない。ヘーズが!係よ)も大きいフィルムでは透
明性が悪く、液晶パネルとし走 7 − ときに1表示された文字1図形、記号等の判読が困難で
ある。また、複屈折率が30X10−3よシ小さいと、
液晶パネルとしたときに干渉縞を生じて判読性を低下さ
せる。しかし複屈折率がl/θ×10′ よりも大ぎく
なると、フィルムがさけ易くなυ、製造時に製品中にス
リットする際とか、液晶パ坏ル板にスリットする原困難
となシ好ましくない。
In addition, the film according to the present invention must have a birefringence of jOXlo-" to /10x10-" with a high flux density. Haze! However, large films have poor transparency, making it difficult to read characters, figures, symbols, etc. displayed on a liquid crystal panel. Also, if the birefringence is smaller than 30X10-3,
When used as a liquid crystal panel, interference fringes occur, reducing readability. However, if the birefringence is larger than 1/θ×10', the film will be difficult to avoid, and it will be difficult to slit it into a product during manufacture or into a liquid crystal panel plate, which is undesirable.

本発明に係るフィルムは、さらに耐熱性のよいことが望
ましい。すなわち液晶パネルの製作に除しては、フィル
ム上への導電被膜の形成その他でフィルムが加熱条件下
におかれることが多いので、加熱によシ透明性が低下し
た91寸法が変化したシしないものであることが望まし
い。実用的見地からは、/!O’Qの雰囲気中に30、
分間保持したときの収縮率が!多収下であp、かつ10
θμの厚さでのヘーズが!多収下であることが望ましい
。本発明者の検討によれば、この条件はフィルムの製造
工程において。
It is desirable that the film according to the present invention further has good heat resistance. In other words, in the production of liquid crystal panels, films are often subjected to heating conditions in order to form a conductive film on the film, etc., so that heating does not cause changes in 91 dimensions that reduce transparency. It is desirable that the From a practical point of view, /! 30 in the atmosphere of O'Q,
The shrinkage rate when held for minutes! p under high yield, and 10
The haze at a thickness of θμ! It is desirable to have high yields. According to the inventor's study, this condition is established in the film manufacturing process.

面配向度か3θX10”−”以上のフィルム全平均屈 
8− 折率がZj 96以上となるように熱処理することによ
り達成される。
The total average refraction of a film with a plane orientation of 3θX10”-” or more
8- Achieved by heat treatment so that the refractive index becomes Zj 96 or more.

以上、詳述したように1本発明に係る液晶パネル基材用
フィルムは、/θ0μの厚さで!多収下のヘーズと30
×10−”〜//θX / 0−”の複屈折率を有して
おシ、これを用いて製作した液晶パネルは見る方向によ
って干渉縞が発生することがなく、かつ判読性にすぐれ
ている。
As detailed above, the film for liquid crystal panel substrate according to the present invention has a thickness of /θ0μ! Haze under high yield and 30
It has a birefringence of ×10-”~//θX/0-”, and liquid crystal panels manufactured using it do not generate interference fringes depending on the viewing direction, and have excellent readability. There is.

以下に実施例によυ本発明をさらに具体的に説明するが
1本発明はその要旨を超えない限9゜以下の実施例に限
定されるものではない。
Hereinafter, the present invention will be explained in more detail with reference to Examples, but the present invention is not limited to the Examples having a diameter of 9° or less unless it exceeds the gist thereof.

なお1本明細書における厚さ斑、熱収縮率。Note: 1. Thickness unevenness and heat shrinkage rate in this specification.

平均屈折率1面配向度、?lJ屈折率、フイルムヘーズ
および干渉縞の測定は下記の方法による。
Average refractive index, degree of one-plane orientation, ? The lJ refractive index, film haze, and interference fringes were measured by the following methods.

(イ)厚み斑 安置電気社製連続フィルム厚さ測定器(電子マイクロメ
ーター使用)によシ、フィルムの主軸方向に沿って一2
711測定し1次式によシ算出した。
(b) Thickness unevenness Using a continuous film thickness measuring device (using an electronic micrometer) made by Anki Denki Co., Ltd., measure the thickness of the film along the main axis direction of the film.
711 was measured and calculated using a linear equation.

(ロ) 熱収縮率 フィルムの玉軸方向およびこれに直角な方向に沿ってそ
れぞれ300g X / j nmの試験片を切り出し
、これを15θ“Cに保持した熱風循環炉にその一端全
挾持して吊り下げ。
(b) Cut out test pieces of 300 g x / j nm each along the ball axis direction of the heat shrinkage film and the direction perpendicular to this, and hold one end of each specimen in a hot air circulation furnace maintained at 15θ"C. Hanging.

30分間熱処理した。熱処理の前後における試験片の長
さ方向の寸法を訓電し1次式により熱収縮率を算出した
Heat treatment was performed for 30 minutes. The longitudinal dimensions of the test piece before and after heat treatment were calculated, and the heat shrinkage rate was calculated using a linear equation.

熱収IF5率−(熱処理前の長さ一熱処理後の長さ)/
熱処理前の長さ×/θO(%ン e→ 平均屈折率、複屈折率および面配向度フィルムの
力n折率の測定は、アタコ゛(1勺製アツベの屈折計全
使用し、光源にはナトリウムランプ金円いて行なった0 フィルム面内の最大の屈折率nM mそれに直角方向の
屈折率nβ及び厚さ方向の屈折率na  を求め、平均
屈折率、被屈折率及び面配向度?次式に従って算出した
Heat recovery IF5 rate - (length before heat treatment - length after heat treatment) /
Length before heat treatment Obtain the maximum refractive index nM in the plane of the film using a sodium lamp, the refractive index nβ in the direction perpendicular to it, and the refractive index na in the thickness direction, and calculate the average refractive index, refractive index, and degree of plane orientation by the following formula: Calculated according to

複屈折率=:nざ−nβ に) フイルムベース ASTM−D−/θ03に準じ1日本嵐色工業社製積分
球式デジタル濁度(輯度)計NDH−20Dによシ求め
た。
Birefringence = nza - nβ) Birefringence was determined using an integrating sphere digital turbidity meter NDH-20D manufactured by Nippon Arashiki Kogyo Co., Ltd. according to film base ASTM-D-/θ03.

7 イ/l/ ムの厚す全d(μ)、フィルムヘースノ
測定値をHImフィルム表面に流動パラフィンを塗布し
た後のヘーズの測定値を4とすると。
7 I/l/ The total thickness of the film d (μ), the measured value of film haze is HIm, and the measured value of haze after applying liquid paraffin to the film surface is assumed to be 4.

100μの厚さのフィルムへ−XHVi下式で定在され
る。
For a film with a thickness of 100μ, -XHVi is determined by the following equation.

(ホ)干渉縞− 偵 一枚の偏光板をまずそれぞれ偏光軸が直交する方向に重
ね、その偏光板の間にフィルムをはさみ、偏光板の偏光
軸とフィルムの玉軸11一 方向が一致するようにする。このような状態で太陽光に
かざし、あらゆる角度からながめた時、干渉による色が
つかないものを良、角度によって色のつくものを不良と
した。
(E) Interference fringes - First, stack one polarizing plate in a direction in which the polarizing axes are perpendicular to each other, then sandwich a film between the polarizing plates so that the polarizing axis of the polarizing plate and the ball axis 11 of the film coincide in one direction. do. When held up to sunlight and viewed from all angles in this condition, those that did not change color due to interference were evaluated as good, and those that changed color depending on the angle were evaluated as poor.

実施例/ ジメチルテレフタレート700部(刀(置部。Example/ 700 parts of dimethyl terephthalate (sword (Okibe).

以下、特記しない限り部はN置部金示す。)。Hereinafter, unless otherwise specified, parts are indicated by N. ).

エチレングリコール30部及び酢酸マグネシウム四水塩
O9θデ部を反応器にとり加熱昇温すると共に、メタノ
ールを留去させ、約グ時間を要して、23θ℃にし、エ
ステル又換反応を終了した。次に、この反応物に、エチ
ルアシドホスフェートθ、04を部および三酸化アンチ
モンθ、o4を部を添加し、常法に従って重合し、比抵
抗が3.0×/θ−70/m のポリエステルチップを
得た。
30 parts of ethylene glycol and 90 parts of magnesium acetate tetrahydrate were placed in a reactor and heated to raise the temperature, and methanol was distilled off, and the temperature was raised to 230° C. over a period of approximately 3 hours to complete the ester conversion reaction. Next, parts of ethyl acid phosphate θ, 04 and parts of antimony trioxide θ, 04 were added to this reaction product, and polymerized according to a conventional method to produce a polyester having a specific resistance of 3.0×/θ-70/m. Got a tip.

このチップを/4θ°0で70時間真空乾燥後。This chip was vacuum dried at /4θ°0 for 70 hours.

λり0 ℃で溶融し、Tダイから押出して静電印加冷却
法にて急冷して3!θμの未延伸フィルムを得喪。この
未延伸フィルムをと7℃で縦方向に3.5倍延伸したこ
のフィルムを横延伸機のレ12− 一ルを真すぐにして延伸がかからないようにしたテンタ
ーに送シ込み22□゛0で70秒間熱固定して、厚さ/
θθμの一軸延伸フイルムを得た。得られたフィルムの
物性を第1表に示した。
Melt at λ = 0 °C, extrude through a T-die, and rapidly cool using the electrostatic cooling method.3! An unstretched film of θμ was obtained. This unstretched film was stretched 3.5 times in the machine direction at 7°C, and then fed into a tenter with the horizontal stretching machine level 12 straight to prevent stretching. Heat set for 70 seconds with
A uniaxially stretched film of θθμ was obtained. The physical properties of the obtained film are shown in Table 1.

比較例/ 厚さ/!θμの未延伸フィルムの縦延伸倍率を/、!倍
とした以外は実施例/と同様にして厚さ700μの一軸
延伸フィルムを得た。このフィルムの物性を第1表に示
す。
Comparative example / Thickness /! The longitudinal stretching ratio of the unstretched film of θμ is /,! A uniaxially stretched film with a thickness of 700 μm was obtained in the same manner as in Example except that the film was doubled. The physical properties of this film are shown in Table 1.

実施例λ 実施例/において、厚さgtθμの未延伸フィルムi 
(+’ 7 ’(lで縦方向に/、!倍延伸し1次いで
10θ℃で横方向に3.3倍延伸したのち。
Example λ In Example/, an unstretched film i having a thickness gtθμ
(+' 7 '(l) after being stretched by /,! times in the machine direction and then 3.3 times in the cross direction at 10θ°C.

220℃で10秒間熱固定して、厚さ/θθμの二軸延
伸フィルムを得た。このフィルムの物性を第1表に示す
The film was heat-set at 220° C. for 10 seconds to obtain a biaxially stretched film having a thickness of /θθμ. The physical properties of this film are shown in Table 1.

実施例3 熱固定を730℃で70秒間行なった以外は。Example 3 Except that heat fixation was performed at 730°C for 70 seconds.

実施例−と同様にして二軸延伸フィルムを得た。A biaxially stretched film was obtained in the same manner as in Example.

このフィルムの物性を第1表に示す。The physical properties of this film are shown in Table 1.

比較例2 実施例/において、/り0θμの未延伸フィルムを?7
°0で縦方向に3.6倍延伸し、次いで700℃で楢方
向に3.2倍延伸したのち、220°0で70秒間熱固
定して厚さ/θオμの二軸延伸フィルムe ?0た。こ
のフィルムの物性ヲ用/表に示す。
Comparative Example 2 In Example/, the unstretched film with /0θμ? 7
After stretching 3.6 times in the machine direction at 0 °C, then stretching 3.2 times in the direction of the oak at 700 °C, heat-setting at 220 °0 for 70 seconds to obtain a biaxially stretched film with a thickness of /θ o μ. ? 0. The physical properties of this film are shown in the table below.

Claims (1)

【特許請求の範囲】 (1)テレフタレートまたは、2,6−ナフタレート系
ポリエステルよシなす、複屈折率が3θ×70−”〜/
lθ×/θ−3でちゃ、かつ/θθμの厚さでのヘーズ
が!係以下であることを特徴とする液晶パネル基材用ポ
リエステルフィルム。 +21  平均屈折率が7.396以上であること全特
徴とする特許請求の範囲第1項記載のポリエステルフィ
ルム0 (3)/!tO℃で3θ分間保持したときの/θθμの
厚さでのヘーズが夕係以下であシ、かつ収縮率が!チ以
下であることを特徴とする特許請求の範囲第1項または
第2項記載のポリエステルフィルム。 (4)面配向度が30×/θ−3以上の一軸または二軸
延伸ポリエステルフィルムf/15’0℃〜2 & j
 ’Oで熱固定したものであること全特徴とする特許請
求の範囲第1項ないし第3項のいずれかに記載のポリエ
ステルフィルム。
[Scope of Claims] (1) Made of terephthalate or 2,6-naphthalate polyester, with a birefringence of 3θ×70−”~/
The haze is lθ×/θ−3 and the thickness is /θθμ! A polyester film for a liquid crystal panel substrate, characterized in that the polyester film has a +21 The polyester film according to claim 1, which is characterized in that the average refractive index is 7.396 or more 0 (3)/! When held at tO℃ for 3θ minutes, the haze at a thickness of /θθμ is less than that, and the shrinkage rate is! 3. The polyester film according to claim 1 or 2, characterized in that the polyester film has a polyester film of less than or equal to (4) Uniaxially or biaxially stretched polyester film with a degree of plane orientation of 30x/θ-3 or more f/15'0°C to 2&j
The polyester film according to any one of claims 1 to 3, wherein the polyester film is heat-set with O.
JP20003782A 1982-11-15 1982-11-15 Polyester film for base material of liquid crystal panel Granted JPS5988719A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20003782A JPS5988719A (en) 1982-11-15 1982-11-15 Polyester film for base material of liquid crystal panel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20003782A JPS5988719A (en) 1982-11-15 1982-11-15 Polyester film for base material of liquid crystal panel

Publications (2)

Publication Number Publication Date
JPS5988719A true JPS5988719A (en) 1984-05-22
JPH0466002B2 JPH0466002B2 (en) 1992-10-21

Family

ID=16417770

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20003782A Granted JPS5988719A (en) 1982-11-15 1982-11-15 Polyester film for base material of liquid crystal panel

Country Status (1)

Country Link
JP (1) JPS5988719A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62135801A (en) * 1985-12-09 1987-06-18 Diafoil Co Ltd Uniaxially highly oriented film comprising polyethylene naphthalate for polarizing plate
JPS62135338A (en) * 1985-12-09 1987-06-18 Diafoil Co Ltd Monoaxially high-orientated film of polyethylene-naphthalate for liquid crystal panel substrate
JPS6342845A (en) * 1986-08-11 1988-02-24 Diafoil Co Ltd Polyester film for liquid crystal indication
US7101627B2 (en) 2001-09-11 2006-09-05 Dupont Teijin Films U.S. Limited Partnership Heat-stabilised poly(ethylene naphthalate) film for flexible electronic and opto-electronics devices
JP2021081743A (en) * 2021-02-22 2021-05-27 凸版印刷株式会社 Light control film, light control device using the same, and screen
JP2021517991A (en) * 2018-04-26 2021-07-29 エルジー・ケム・リミテッド Optical devices and their uses

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2009166442A (en) * 2008-01-18 2009-07-30 Mitsubishi Plastics Inc Method for producing uniaxially oriented polyester film

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5697318A (en) * 1980-01-07 1981-08-06 Hitachi Ltd Liquid-crystal display element
JPS5711319A (en) * 1980-06-23 1982-01-21 Toyobo Co Ltd Transparent conductive film for liquid crystal display device
JPS57118220A (en) * 1981-01-13 1982-07-23 Toyobo Co Ltd Polarizing plate having transparent conductive layer
JPS57128319A (en) * 1981-02-02 1982-08-09 Hitachi Ltd Display panel

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5697318A (en) * 1980-01-07 1981-08-06 Hitachi Ltd Liquid-crystal display element
JPS5711319A (en) * 1980-06-23 1982-01-21 Toyobo Co Ltd Transparent conductive film for liquid crystal display device
JPS57118220A (en) * 1981-01-13 1982-07-23 Toyobo Co Ltd Polarizing plate having transparent conductive layer
JPS57128319A (en) * 1981-02-02 1982-08-09 Hitachi Ltd Display panel

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62135801A (en) * 1985-12-09 1987-06-18 Diafoil Co Ltd Uniaxially highly oriented film comprising polyethylene naphthalate for polarizing plate
JPS62135338A (en) * 1985-12-09 1987-06-18 Diafoil Co Ltd Monoaxially high-orientated film of polyethylene-naphthalate for liquid crystal panel substrate
EP0228611A3 (en) * 1985-12-09 1988-08-03 Diafoil Company, Limited Uniaxially high-oriented polyethylene naphthalate film for polarizing plates
US4799772A (en) * 1985-12-09 1989-01-24 Diafoil Company, Limited Uniaxially high-oriented polyethylene naphthalate film for liquid crystal panel substrates
JPS6342845A (en) * 1986-08-11 1988-02-24 Diafoil Co Ltd Polyester film for liquid crystal indication
US7101627B2 (en) 2001-09-11 2006-09-05 Dupont Teijin Films U.S. Limited Partnership Heat-stabilised poly(ethylene naphthalate) film for flexible electronic and opto-electronics devices
US7300703B2 (en) 2001-09-11 2007-11-27 Dupont Teijin Films U.S. Limited Partnership Heat-stabilised poly(ethylene naphthalate) film for flexible electronic and opto-electronic devices
JP2021517991A (en) * 2018-04-26 2021-07-29 エルジー・ケム・リミテッド Optical devices and their uses
US11428968B2 (en) 2018-04-26 2022-08-30 Lg Chem, Ltd. Optical device and use thereof
JP2021081743A (en) * 2021-02-22 2021-05-27 凸版印刷株式会社 Light control film, light control device using the same, and screen

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